Contrasting the development of larval and adult body plans during the evolution of biphasic lifecycles in sea urchins.

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Development Pub Date : 2024-10-15 Epub Date: 2024-10-28 DOI:10.1242/dev.203015
Brennan D McDonald, Abdull J Massri, Alejandro Berrio, Maria Byrne, David R McClay, Gregory A Wray
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Abstract

Biphasic lifecycles are widespread among animals, but little is known about how the developmental transition between larvae and adults is regulated. Sea urchins are a unique system for studying this phenomenon because of the stark differences between their bilateral larval and pentaradial adult body plans. Here, we use single-cell RNA sequencing to analyze the development of Heliocidaris erythrogramma (He), a sea urchin species with an accelerated, non-feeding mode of larval development. The sequencing time course extends from embryogenesis to roughly a day before the onset of metamorphosis in He larvae, which is a period that has not been covered by previous datasets. We find that the non-feeding developmental strategy of He is associated with several changes in the specification of larval cell types compared to sea urchins with feeding larvae, such as the loss of a larva-specific skeletal cell population. Furthermore, the development of the larval and adult body plans in sea urchins may utilize largely different sets of regulatory genes. These findings lay the groundwork for extending existing developmental gene regulatory networks to cover additional stages of biphasic lifecycles.

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对比海胆双相生命周期进化过程中幼体和成体体型的发展。
双相生命周期在动物中非常普遍,但人们对幼体和成体之间的发育过渡是如何调节的却知之甚少。海胆是研究这一现象的独特系统,因为它们的双侧幼体和五侧成体身体计划之间存在明显差异。在这里,我们利用单细胞 RNA 测序技术分析了红海胆(Heliocidaris erythrogramma,He)的发育过程,红海胆是一种幼体发育加速、非进食模式的海胆。测序的时间过程从胚胎发生一直延伸到氦海胆幼体开始变态前大约一天,这是以前的数据集没有涵盖的时期。我们发现,与有进食幼体的海胆相比,He 的非进食发育策略与幼体细胞类型规格的几种变化有关,例如幼体特异性骨骼细胞群的缺失。此外,海胆幼体和成体的发育可能利用了大体不同的调控基因。这些发现为扩展现有的发育基因调控网络以涵盖双相生命周期的更多阶段奠定了基础。
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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
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